HYDROXYCHLOROQUINE SULFATE
- Product NDC
- 59746-780
- 11-digit product format
- 597460780
- Labeler code
- 59746
- Product ID
- 59746-780_633162d7-2dca-4584-a374-cf4d7ee0b7a8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- hydroxychloroquine sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Jubilant Cadista Pharmaceuticals Inc.
- Application
- ANDA212902
- Marketing category
- ANDA
- Marketing start
- 2020-07-22
- Marketing end
- 0000-00-00
- Substance
- HYDROXYCHLOROQUINE SULFATE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Antimalarial [EPC], Antirheumatic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59746-780-01 | 59746078001 | 100 TABLET in 1 BOTTLE (59746-780-01) | 100 tablet | 2020-07-25 | 0000-00-00 | No | No | Current |
| 59746-780-05 | 59746078005 | 500 TABLET in 1 BOTTLE (59746-780-05) | 500 tablet | 2020-07-25 | 0000-00-00 | No | No | Current |